-
1
-
-
85014698029
-
Evidence-based strategies for shortening informed consent forms in clinical research
-
Corneli, A., E., Namey, M. P., Mueller, J., Tharaldson, S., Sortijas, T., Grey, and J., Sugarman. 2017. Evidence-based strategies for shortening informed consent forms in clinical research. Journal of Empirical Research on Human Research Ethics 12 (1):14–25.
-
(2017)
Journal of Empirical Research on Human Research Ethics
, vol.12
, Issue.1
, pp. 14-25
-
-
Corneli, A.1
Namey, E.2
Mueller, M.P.3
Tharaldson, J.4
Sortijas, S.5
Grey, T.6
Sugarman, J.7
-
2
-
-
85021741894
-
Reducing consent form length: Stakeholder support, evidence-based strategies, and regulatory requirements
-
Corneli, A., and J., Sugarman. 2017. Reducing consent form length:Stakeholder support, evidence-based strategies, and regulatory requirements. IRB:Ethics & Human Research 39 (2):18–20.
-
(2017)
IRB: Ethics & Human Research
, vol.39
, Issue.2
, pp. 18-20
-
-
Corneli, A.1
Sugarman, J.2
-
3
-
-
84891667429
-
Patients’ attitudes toward the donation of biological materials for the derivation of induced pluripotent stem cells
-
Dasgupta, I., J., Bollinger, D. J. H., Mathews, N., Neumann, A., Rattani, and J., Sugarman. 2014. Patients’ attitudes toward the donation of biological materials for the derivation of induced pluripotent stem cells. Cell Stem Cell 14:9–12.
-
(2014)
Cell Stem Cell
, vol.14
, pp. 9-12
-
-
Dasgupta, I.1
Bollinger, J.2
Mathews, D.J.H.3
Neumann, N.4
Rattani, A.5
Sugarman, J.6
-
4
-
-
34147101837
-
Improving informed consent: suggestions from parents of children with leukemia
-
Eder, M. L., A. D., Yamokoski, P. W., Wittmann, and E. D., Kodish. 2007. Improving informed consent:suggestions from parents of children with leukemia. Pediatrics 119 (4):e849–59.
-
(2007)
Pediatrics
, vol.119
, Issue.4
, pp. e849-e859
-
-
Eder, M.L.1
Yamokoski, A.D.2
Wittmann, P.W.3
Kodish, E.D.4
-
5
-
-
4644281540
-
Interventions to improve research participants' understanding in informed consent for research: A systematic review. Review
-
Flory, J., and E., Emanuel. 2004. Interventions to improve research participants' understanding in informed consent for research:A systematic review. Review. Journal of the American Medical Association 292 (13):1593–601.
-
(2004)
Journal of the American Medical Association
, vol.292
, Issue.13
, pp. 1593-1601
-
-
Flory, J.1
Emanuel, E.2
-
6
-
-
85021752827
-
-
Washington, DC: National Academies Press
-
IOM (Institute of Medicine). 2015. Informed consent and health literacy:Workshop summary. Washington, DC:National Academies Press. Available at:http://www.nationalacademies.org/hmd/Reports/2015/Informed-Consent-Health-Literacy.aspx
-
(2015)
Informed consent and health literacy: Workshop summary
-
-
-
7
-
-
67649917702
-
Purpose and benefits of early phase cancer trials: What do oncologists say? What do patients hear?
-
Kass, N., H., Taylor, L., Fogarty, J., Sugarman, S. N., Goodman, A., Goodwin-Landher, M., Carducci, and H., Hurwitz. 2008. Purpose and benefits of early phase cancer trials:What do oncologists say? What do patients hear? Journal of Empirical Research on Human Research Ethics 3:57–68.
-
(2008)
Journal of Empirical Research on Human Research Ethics
, vol.3
, pp. 57-68
-
-
Kass, N.1
Taylor, H.2
Fogarty, L.3
Sugarman, J.4
Goodman, S.N.5
Goodwin-Landher, A.6
Carducci, M.7
Hurwitz, H.8
-
8
-
-
0033119358
-
Improving informed consent in clinical trials: A duty to experiment
-
Lavori, P. W., J., Sugarman, M. T., Hays, and J. R., Feussner. 1999. Improving informed consent in clinical trials:A duty to experiment. Controlled Clinical Trials 20 (2):187–93.
-
(1999)
Controlled Clinical Trials
, vol.20
, Issue.2
, pp. 187-193
-
-
Lavori, P.W.1
Sugarman, J.2
Hays, M.T.3
Feussner, J.R.4
-
9
-
-
84942943428
-
Use of altered informed consent in pragmatic clinical research
-
McKinney, R. E., Jr., L. M., Beskow, D. E., Ford, et al. 2015. Use of altered informed consent in pragmatic clinical research. Clinical Trials 12:494–502.
-
(2015)
Clinical Trials
, vol.12
, pp. 494-502
-
-
McKinney, R.E.1
Beskow, L.M.2
Ford, D.E.3
-
10
-
-
85021721094
-
Federal policy for the protection of human subjects
-
Office of Human Research Protections. 2017. Federal policy for the protection of human subjects. Federal Register 82 (12):7149–7274.
-
(2017)
Federal Register
, vol.82
, Issue.12
, pp. 7149-7274
-
-
-
11
-
-
0001890859
-
Empirical research on informed consent
-
Sugarman, J., D. C., McCrory, D., Powell, et al. 1999. Empirical research on informed consent. Hastings Center Report 29:S1–S42.
-
(1999)
Hastings Center Report
, vol.29
, pp. S1-S42
-
-
Sugarman, J.1
McCrory, D.C.2
Powell, D.3
-
12
-
-
34147213973
-
Formative research in clinical trial development: Attitudes of patients with arthritis in enhancing prevention trials
-
Taylor, H. A., J., Sugarman, D. S., Pisetsky, and J., Bathon. 2007. Formative research in clinical trial development:Attitudes of patients with arthritis in enhancing prevention trials. Annals of the Rheumatic Diseases 66 (4):542–4.
-
(2007)
Annals of the Rheumatic Diseases
, vol.66
, Issue.4
, pp. 542-544
-
-
Taylor, H.A.1
Sugarman, J.2
Pisetsky, D.S.3
Bathon, J.4
-
13
-
-
85021736965
-
-
(accessed 30 May 2017)
-
US Congress. H.R. 34–1114th Congress (2015–2016). 21st Century Cures Act. Title II, Subtitle C, Section 3023. Protection of Human Subjects. Available at:https://www.congress.gov/114/bills/hr34/BILLS-114hr34enr.pdf (accessed 30 May 2017).
-
-
-
-
14
-
-
84995543060
-
Trial reporting in clinicaltrials.gov—The final rule
-
Zarin, D. A., T., Tse, R. J., Williams, and S., Carr. 2016. Trial reporting in clinicaltrials.gov—The final rule. New England Journal of Medicine 375 (20):1998–2004.
-
(2016)
New England Journal of Medicine
, vol.375
, Issue.20
, pp. 1998-2004
-
-
Zarin, D.A.1
Tse, T.2
Williams, R.J.3
Carr, S.4
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